Variant #0000569004 (NC_000020.10:g.10030704T>A, NM_130811.2:c.-168985T>A (SNAP25))

Chromosome 20
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.10030704T>A
DNA change (hg38) g.10050056T>A
Published as ANKEF1(NM_022096.4):c.1487T>A (p.(Ile496Asn))
ISCN -
DB-ID SNAP25_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ANKEF1 NM_022096.4 ?/. - c.1487T>A r.(?) p.(Ile496Asn)
SNAP25 NM_130811.2 ?/. - c.-168985T>A r.(?) p.(=)
SNAP25-AS1 NR_040710.1 ?/. - n.500-23408A>T r.(?) -


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